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The overall aim of this review is to summarize recent advances in studies of AD progression and the use of animal models in gene expression studies of AD progression.
In this paper, two models in gene expression programming (GEP) approach for predicting compressive strength of concretes containing rice husk ash have been developed at the age of 1, 3, 7, 14, 28, 56 and 90 days.
Any discussion of DMD models in gene therapy that lacked mention of mdx mice would not be complete.
Therefore, scaffolds smaller than 2 kbp were skipped in order to reduce the false positive errors and fragmented gene models in gene prediction.
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P. berghei is the most frequently used malaria parasite model in gene function analysis since phenotype screens throughout the complete Plasmodium life cycle are possible both in vitro and in vivo.
Analysis of these differences revealed novel bona fide ABC transporters (Figure 5), as well as defective gene models in current gene annotations of Caenorhabditis genomes.
According to the model, in genes with very low binding to NRSF, a moderate increase of NRSF levels would not alter repressor binding appreciably.
Similarly to the experimentally determined structures, the distribution of selected sites was not random (χ test: P < 0.00001 where P s ≥ 0.9 and P = 0.000176 where P s ≥ 0.99, using the M8 model in genes with a significant M7/M8 LRT).
These gene sets were enriched in our analysis, which supported the suitability of primary cell culture models in studying gene expression in chondrocytes.
But the analysis is nonetheless an example of how Fourier analysis may help in model selection in gene regulation science.
We are currently integrating mouse data, as mice are often used as a model organism in gene hunting.
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